Opto Global, Inc. is one of 24544 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Opto Global, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OPTO GLOBAL DIGITAL FUNDUS CAMERA SYSTEM MODEL ADS 1.5
1
Total
1
Cleared
0
Denied
Opto Global, Inc. has 1 FDA 510(k) cleared medical devices. Based in Granite Bay, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Opto Global, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Opto Global, Inc.
1 devices